JPS5850548A - Electrostatic image developing method - Google Patents
Electrostatic image developing methodInfo
- Publication number
- JPS5850548A JPS5850548A JP56150147A JP15014781A JPS5850548A JP S5850548 A JPS5850548 A JP S5850548A JP 56150147 A JP56150147 A JP 56150147A JP 15014781 A JP15014781 A JP 15014781A JP S5850548 A JPS5850548 A JP S5850548A
- Authority
- JP
- Japan
- Prior art keywords
- image
- polarity
- developer
- developing
- electrostatic latent
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
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- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- NISZMWZPLJGKCC-UHFFFAOYSA-N lissamine flavine FF free acid Chemical compound C1=CC(C)=CC=C1N(C1=O)C(=O)C2=C3C1=CC=CC3=C(N)C(S(O)(=O)=O)=C2 NISZMWZPLJGKCC-UHFFFAOYSA-N 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- 230000005415 magnetization Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- CTIQLGJVGNGFEW-UHFFFAOYSA-L naphthol yellow S Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C([O-])=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 CTIQLGJVGNGFEW-UHFFFAOYSA-L 0.000 description 1
- 229910000480 nickel oxide Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 description 1
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- WOTPFVNWMLFMFW-ISLYRVAYSA-N para red Chemical compound OC1=CC=C2C=CC=CC2=C1\N=N\C1=CC=C(N(=O)=O)C=C1 WOTPFVNWMLFMFW-ISLYRVAYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- FZUOVNMHEAPVBW-UHFFFAOYSA-L quinoline yellow ws Chemical compound [Na+].[Na+].O=C1C2=CC=CC=C2C(=O)C1C1=NC2=C(S([O-])(=O)=O)C=C(S(=O)(=O)[O-])C=C2C=C1 FZUOVNMHEAPVBW-UHFFFAOYSA-L 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 150000003342 selenium Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- KVMUSGMZFRRCAS-UHFFFAOYSA-N sodium;5-oxo-1-(4-sulfophenyl)-4-[(4-sulfophenyl)diazenyl]-4h-pyrazole-3-carboxylic acid Chemical compound [Na+].OC(=O)C1=NN(C=2C=CC(=CC=2)S(O)(=O)=O)C(=O)C1N=NC1=CC=C(S(O)(=O)=O)C=C1 KVMUSGMZFRRCAS-UHFFFAOYSA-N 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000003351 stiffener Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- JADVWWSKYZXRGX-UHFFFAOYSA-M thioflavine T Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C1=[N+](C)C2=CC=C(C)C=C2S1 JADVWWSKYZXRGX-UHFFFAOYSA-M 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000013518 transcription Methods 0.000 description 1
- 230000035897 transcription Effects 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- JEVGKYBUANQAKG-UHFFFAOYSA-N victoria blue R Chemical compound [Cl-].C12=CC=CC=C2C(=[NH+]CC)C=CC1=C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 JEVGKYBUANQAKG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/01—Electrographic processes using a charge pattern for multicoloured copies
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Dry Development In Electrophotography (AREA)
- Magnetic Brush Developing In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、静電潜侭の現像法に係るもので、%に多色画
像の現像法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrostatic latent development method, particularly to a multicolor image development method.
静電潜傷を多色画像で表わす典型的なものは電子写真方
式を用いたカラー画像に関するものである。A typical example of representing electrostatic latent scratches in a multicolor image is a color image using an electrophotographic method.
とれKはオリジナル原稿に光フィルターを通して色分解
し、この分解光を露光として用い、帯電露光、現像、転
写の工程を、イエロー色、マゼンタ色、シアン色、黒色
の各着色トナーによる現像を組み合わせ、次々と4回繰
り返すことにより行なわれる。その他にも、同一感光体
上に異極性の静電潜像を作成し、黒色と赤色トナーによ
り現像する方法がある。Tore K passes the original document through an optical filter to separate the colors, uses this separated light as exposure, and combines the steps of charging exposure, development, and transfer with development using yellow, magenta, cyan, and black colored toners. This is done by repeating it one after another four times. Another method is to create electrostatic latent images of different polarities on the same photoreceptor and develop them with black and red toners.
これらの多色画像は白黒の情報と比べ色による情報をも
付加できるためKgましいものではあるが、通常各色に
対応して現像6を用いる必要があるため、
(1) 機械が大型になり、コストが高くナル。These multicolor images are advantageous because they can add color information compared to black and white information, but because it is usually necessary to use a developer 6 for each color, (1) the machine becomes larger; , high cost and null.
(2) 反覆動作による色ずれ精度の保証が必要とな
る。(2) It is necessary to guarantee color misregistration accuracy through repeated operations.
0) 一枚のコピ一時間が長くなる。0) It takes an hour longer to copy one sheet.
といった問題がある。There are problems like this.
このことから、同一現像器内に色の異なる2色の現像剤
を混合し、これ罠よって現像装置をコンパクトにする試
みが行なわれている(例えば特公昭55−30625号
公報)が、上記引用例で用いている色の異なる2色の現
像剤の単なる混合だけでは以下のような欠点を生じる。For this reason, attempts have been made to make the developing device more compact by mixing two different color developers in the same developing device (for example, Japanese Patent Publication No. 55-30625); Mere mixing of two different color developers used in the example causes the following drawbacks.
α) 静電潜像がない部分でも現像が起こる、すなわち
かぶりを生じる。α) Development occurs even in areas where there is no electrostatic latent image, that is, fogging occurs.
(2) 現像した画像を構成する現像剤に他の現像剤
が混入するため色が悪い、すなわち色にごりが発生する
。(2) Other developers are mixed into the developer constituting the developed image, resulting in poor color, that is, color turbidity.
子を使用して現像した時、かぶりの発生のない静電荷像
現像方法を提供することである・本発明の他の目的は、
互いに異なる帯電極性を有する着色粒子を使用して現像
した時、色にごりの発生しない静電荷gI現偉方法を提
供することである。Another object of the present invention is to provide a method for developing an electrostatic image that does not cause fogging when developed using a photocoat.
It is an object of the present invention to provide a method for developing electrostatic charge gI that does not cause color clouding when color particles having different charge polarities are used for development.
さらに本発明の他の目的は、互いKJ%なる帯電極性を
有する着色粒子を使用して現像した時、鮮鋭な画像が得
られる静電荷像現像方法を提供することである。Still another object of the present invention is to provide an electrostatic image developing method that can produce sharp images when developed using colored particles having charge polarities KJ% of each other.
本発明の上記諸目的は、互いKffなる帯電極性を有す
る着色粒子から一方の極性に帯電された着色粒子と選択
的に抽出し、抽出された着色粒子で儂支持体の真なる極
性の静電潜像の一方の極性の静電潜像を現像することを
特徴とする静電荷像現像方法により達成される。The above-mentioned objects of the present invention are to selectively extract colored particles charged to one polarity from colored particles having charged polarities Kff to each other, and use the extracted colored particles to absorb the true polarity of the electrostatic charge of the support. This is achieved by an electrostatic image developing method characterized by developing an electrostatic latent image of one polarity of the latent image.
互いに異なる帯電極性を有する着色粒子(以下複合現像
剤と称する)を用い現像する際における問題の1つは現
像剤が非画像部にも付着し、発生するかぶりの問題であ
る。One of the problems in developing using colored particles having different charging polarities (hereinafter referred to as composite developer) is the problem of fogging caused by the developer adhering to non-image areas.
以下この問題を図面を用い^体的に説明する。This problem will be explained below using drawings.
第1図は静電潜像の電位と現像に寄与する現像剤量との
関係を示すものであり、横軸は静電潜像の電位を、たて
軸は@偉に寄与する現像剤の量を示す。曲線Iは正電位
の静電潜像に付着する負帯電現像剤量を表わし、曲線■
は負電位の静電潜像に付着する正帯電現像量を表わす。Figure 1 shows the relationship between the potential of the electrostatic latent image and the amount of developer contributing to development. The horizontal axis represents the potential of the electrostatic latent image, and the vertical axis represents the amount of developer contributing to the development. Indicate quantity. Curve I represents the amount of negatively charged developer that adheres to the electrostatic latent image with positive potential, and curve ■
represents the amount of positively charged development that adheres to a negative potential electrostatic latent image.
gi図において、斜線部分■はかぶりのS分を示す。こ
の発生したかぶりを除去すべく単に電気的バイアスな現
像剤支持体(例えば現像スリーブ)K印加すると、こん
どは逆極性のam剤が偉支持体に付着し、かぶりが発生
する。すなわち、電気的バイアスによってはかぶりを除
去できない。In the gi diagram, the shaded area ■ indicates the S portion of the fog. If an electrical bias K is simply applied to a developer support (for example, a developing sleeve) in order to remove the generated fog, then the am agent of the opposite polarity will adhere to the support and fog will occur. That is, the fog cannot be removed by electrical bias.
そこで、選択的に一方の現像剤のみを抽出する手段を設
け、抽出された3J儂剤を従来の一成分現像剤に対して
用いられる方法によって!I像することによりかぶり発
生の問題を解決することができる。Therefore, a means for selectively extracting only one of the developers was provided, and the extracted 3J developer was extracted using the method used for conventional one-component developers! By performing an I-image, the problem of fogging can be solved.
以下図面を用いて本発明の詳細な説明する。第2図にお
いて、lはその表面に光導電体を設けた感光体ドラム、
2は現像器を示す。IA倫器2は、現像ローラ2−bと
供給ローラ2−aで構成されて感光体ドラムl、現像ロ
ーラ2−b、供給ローラ2−aはそれぞれ矢印方向忙回
転する。尚、醜2図中、eおよびθはプラスおよびマイ
ナスに帯電された着色粒子を示す。探電した複合現像剤
を供給ローラ2−aは誼ローラの回転とその内部の一定
磁石の作用により、#ローラから現像ローラ2−b上へ
と特定の極性をもっ現像剤のみを電気的手段すなわち、
直流電圧の印加により移動させる。The present invention will be described in detail below using the drawings. In FIG. 2, l is a photosensitive drum with a photoconductor provided on its surface;
2 indicates a developing device. The IA converter 2 is composed of a developing roller 2-b and a supply roller 2-a, and the photosensitive drum 1, the developing roller 2-b, and the supply roller 2-a each rotate in the direction of the arrow. Note that in Figure 2, e and θ indicate positively and negatively charged colored particles. The roller 2-a that supplies the detected composite developer electrically supplies only the developer with a specific polarity from the # roller onto the developing roller 2-b by the rotation of the roller and the action of a certain magnet inside it. That is,
Move by applying DC voltage.
供給a−52−aから現像ローラ2−bへtDQ儂剤の
移動量と電気的手段により印加される電圧との関係はa
I1図と類似したものとなり特定の現像剤のみを移動さ
せるにはある大きさ以上の電位差(zooV〜tKV)
を設ける必要がある。The relationship between the amount of movement of the tDQ agent from the supply a-52-a to the developing roller 2-b and the voltage applied by electrical means is a.
It is similar to Figure I1, and in order to move only a specific developer, a potential difference of a certain magnitude or more (zooV ~ tKV) is required.
It is necessary to provide
この移動を確実にするには、供給□ローラ2−a上の現
像剤な接触以外に9IJえは飛翔させて現像ローラ2−
b上へと移動させる。又は複合現像剤の片方、あるいは
両者共に磁性体を含有させることが有効である。この時
の磁性体の含有量は、有色特に後者は複合現像剤の摩擦
帯電、搬送、飛散防止等rtJIl実に行なうJ:Lが
できる。又、複合現像剤の移動は、不!ll!な極性を
含んだ小塊のまま起こる場合があり、これに対しては第
2図における直流電圧に交番電界を重畳させると、複合
現像剤の凝集がほぐされ特定の現像剤のみをより容易に
移動させることができる。In order to ensure this movement, in addition to contacting the developer on the supply roller 2-a, the 9IJ should be allowed to fly.
b Move it up. Alternatively, it is effective to include a magnetic material in one or both of the composite developers. The content of the magnetic material at this time is such that the latter can be used to effectively perform triboelectrification, transport, prevention of scattering, etc. of the composite developer. Also, the movement of the composite developer is prohibited! ll! In some cases, small lumps containing different polarities are generated, and for this, when an alternating electric field is superimposed on the DC voltage shown in Figure 2, the agglomeration of the composite developer is loosened and only a specific developer can be more easily removed. It can be moved.
現像時にこの交番電界を印加した状態で現像する現像方
法は、静電潜像と現像体担時体上に保持した現像剤を間
陣をおいて対持させ、交番電界下で現像する方法(例え
ば、特開昭55−18656号、同昭55−18657
号、同昭55−18658号、同昭55−18659号
各公報ζ米国特許第3,890,929号明細書) ;
静□電潜像と現像剤を接触状態にし、低周波の交番電界
下で現像する方法が代表的である。これらの技術は現像
剤なRNあるいは振動させることにより、静電潜録に付
着すべき極性の現像剤のみを確実に付着させることがで
きる。又、交番電界の使用は画像の鮮鋭化にも優れた効
果を春Tる・正又は負の静電潜像は同色の複合現像剤に
よって現像してもよいが静電潜像の極性に応じてaなっ
た色をもつ複合現像剤を用いて現像してもよい。A developing method in which the electrostatic latent image and the developer held on the developer carrier are opposed to each other with a space between them and developed under an alternating electric field ( For example, JP-A-55-18656 and JP-A-55-18657.
No. 18658, No. 18658, No. 18659, US Pat. No. 3,890,929);
A typical method is to bring an electrostatic latent image into contact with a developer and develop under a low-frequency alternating electric field. These techniques make it possible to reliably attach only the polar developer to be attached to the electrostatic latent recording material by applying RN or vibration to the developer. In addition, the use of an alternating electric field has an excellent effect on sharpening the image.Positive or negative electrostatic latent images may be developed with a composite developer of the same color, but depending on the polarity of the electrostatic latent image, Developing may be performed using a composite developer having a different color.
このことによりより多くの情報を得ることができる。又
、現像工程は、一方の極性に帯電された現像剤による現
像を順次繰り返してもよいが、両極性の静電潜像を保持
させることができる場合は複合現像剤により同時に現像
することが効率的である。このようにするには装置上の
構成f/jll!3図のようにすればよい。This allows more information to be obtained. In addition, in the development process, development using a developer charged to one polarity may be repeated sequentially, but if it is possible to retain electrostatic latent images of both polarities, simultaneous development using a composite developer is more efficient. It is true. To do this, the configuration on the device f/jll! You can do it as shown in Figure 3.
fE3図において、lは感光体、2は現像器を示す。現
像器2は2つの現像ローラ2−b、2−oを設け、各々
の現像ローラに14なる極性の現像剤な保持するように
しである。又2−&は供給ローラを示し、感光体11現
像ローツ2−b、2−o供給ローラ2−aは各々矢印方
向に回転する。In the fE3 diagram, l indicates a photoreceptor and 2 indicates a developing device. The developing device 2 is provided with two developing rollers 2-b and 2-o, each of which holds a developer having a polarity of 14. Further, 2-& indicates a supply roller, and the photoreceptor 11 developing roller 2-b and 2-o supply roller 2-a each rotate in the direction of the arrow.
感光体1上の両極性の静電潜像【現像ローラ2−b、2
−aで各々異極性の静1!潜像t−現像する。Bipolar electrostatic latent image on photoreceptor 1 [developing rollers 2-b, 2
-A with different polarity static 1! Latent image t - Develop.
現像は通常−成分現像に用いられる手段、丁なわち予め
現像ローラ上に形成された現像剤と静電潜像とが接触す
る条件で行なわれる接触現像法あるいは接触しない非接
触現像が用いられる。又−現像時に現像剤が磁性体を含
む場合は、磁界下で現像を行なうことが有効である。The development is carried out by the means normally used for component development, ie, the contact development method in which the electrostatic latent image is brought into contact with the developer previously formed on the development roller, or the non-contact development method in which no contact is made. Furthermore, when the developer contains a magnetic substance during development, it is effective to carry out the development under a magnetic field.
以上のような現像方法に用いられる現像剤−ハ両極性の
現像剤とも!A極性で同程度の静電潜像電位【有して現
像するために両者の特徴は帯電極性な除き類似したもの
であることが好ましい。このことから両者とも5〜20
μの粒径、0.2〜20 /1 c / Hの帯電量の
大きざ、同様な磁化の強さ、同様72誘電率等の条件が
i、げられよう、又磁性体を含む着色現像剤の製造法と
しては、例えば特開昭51−42539号、同昭53−
118051号、同昭53−118053号各公報の技
術を適用することができる。The developer used in the above development method is also called a bipolar developer! In order to develop the image with the same electrostatic latent image potential of A polarity, it is preferable that the characteristics of both the images are similar except for the charging polarity. From this, both are 5-20
Conditions such as a particle size of μ, a charge amount difference of 0.2 to 20/1 c/H, a similar magnetization strength, and a similar dielectric constant of 72 may be obtained. As a method for producing the agent, for example, JP-A-51-42539 and JP-A-53-
The techniques disclosed in Publications No. 118051 and No. 53-118053 can be applied.
以ド1本発明で用いらnる複合現像剤【説明する。The composite developer used in the present invention will be explained below.
本弗明の複合現像剤は、マイクロカプセル現像剤と粉体
現像剤に大別される。Honyumei's composite developers are broadly divided into microcapsule developers and powder developers.
前者のマイクロカプセル現像剤は一般的に芯物質の外側
に合成樹脂の膜があり、少なくともそのどちらか一万に
磁性体が含まれているものである。The former type of microcapsule developer generally has a synthetic resin film on the outside of a core material, and at least one of the films contains a magnetic material.
特に好ましいのは、芯物質の外側にフィルム形成性高分
子物質を主体とする第1の壁膜が設けられ、さらにその
第1の壁膜の外i1に磁性体を含み合成樹脂を主体とす
る1112の壁膜が設けられている現像剤である。その
カプセル化法には、公知のマイクロカプセル化方法、例
えば、コンプレックスコアセルベージ糟ン法;シンプル
コアセルページ■ス法;ツル)コアセルベージ曽ン法p
pH変化、溶媒変化、溶媒除去によるポリ!−の不溶化
等の水溶性又は水性分散液からの相分離法;界面重合法
; In 8itu重合法などがあるが、ここでは一般
的な方法であるコンプレックスコア七ルペーシ履ン法に
ついて以下に述べる。Particularly preferably, a first wall film mainly made of a film-forming polymer material is provided on the outside of the core material, and further, the outside i1 of the first wall film contains a magnetic material and is mainly made of synthetic resin. This is a developer provided with a 1112 wall film. The encapsulation method includes known microencapsulation methods, such as the complex coacelvage method; the simple coacelvage method;
Poly! by pH change, solvent change, and solvent removal! - Phase separation methods from water-soluble or aqueous dispersions such as insolubilization; interfacial polymerization methods;
所定のpH(アルカリ側)、濃度および温度に調整され
たフィルム形成性高分子物質(例えば、7ラビ7ゴム)
の水溶液に着色剤の非水溶液又は非水分散液【加え分数
乳化せしめ、これに同じpus濃度および温度に調整さ
れたゲル化しつる等電コロイドであるフィルム形成性高
分子物質(例えば、ゼラチン)の水溶液を加える・次に
この混合液のPMを酸性にし相分離を起こさせる。こう
することによって、着色剤の非水溶液又は非水分散液の
液滴の肩りに前記内高分子物質が析出するから、次に!
t−冷却し1硬化剤(ホクマリン)を加えフルカリ性に
して液温を上昇させて析出物を硬化せしめる。さらに、
得られたカプセル液に少なくとも磁性粒子、合成樹脂エ
マルジーンを加え、均一−に分散した後、噴射乾燥する
ことによって目的とするトナーが得られる。Film-forming polymeric substance (e.g. 7 Ravi 7 rubber) adjusted to a predetermined pH (alkaline side), concentration and temperature
A non-aqueous solution or non-aqueous dispersion of the colorant is added to the aqueous solution for fractional emulsification, and to this is added a film-forming polymeric material (e.g. gelatin) which is a gelling and isoelectric colloid adjusted to the same concentration and temperature. Add an aqueous solution.Next, make the PM of this mixture acidic to cause phase separation. By doing this, the inner polymer substance is precipitated on the shoulders of the droplets of the non-aqueous solution or dispersion of the colorant, so next!
After cooling, a curing agent (Hokumarin) is added to make the solution fully caustic and the temperature of the solution is raised to harden the precipitate. moreover,
The desired toner is obtained by adding at least magnetic particles and a synthetic resin emulgene to the obtained capsule liquid, uniformly dispersing the mixture, and then spray drying the mixture.
芯物質に用いられる着色剤としては無機顔料、有機顔料
、直接染料、酸性染料、塩基性染料、媒染、酸性媒染染
料、分散染料、油溶染料などがあげられる。これの具体
例には、
黒色顔料として、カーボンブラック、アセチレンブラッ
ク、ラレプブラック、黒船、ミネラルブラック、アニリ
ンブラック、シアニンブラックなど、
黄色顔料として、黄鉛、亜鉛黄、り胃ム酸バリウム、カ
ドミニウムエロー、鉛−シアナミド1鉛酸カルシウム〜
す7トールエo −B 、へンザエロー3G、ハンザエ
ロー〇、ハシサエローGR,ハンザエローム、ハンザエ
ロA−′RM1ハンザエロー31ピグメントエローL1
ベンジンエロー、ベンジンエロー01ベンジンエローO
R,パーマネントエローNoG %パルカン7アスドエ
ロー501パルカン7アストエローR1タートラジンレ
ーキ、キノリンエ四−レーキ、アシッドイエロー5GL
sパーマネントエロ−?GL 、パーマネントエロー
田(至)、パーマネントエローHR1アンスラビリ之ジ
ンエローなど1
赤色顔料として、ベンガラ、鉛丹、鎖朱、カドミウムレ
ッド、パーマネントレッド411に、パラレッド、ファ
イヤーレッド−洋朱、パラクロルオル)二) vs 7
x−リンレッド1リソールフアスシスカーレツトG1
ブリリアント7アスシスカーレツト、プリリ7ントヵー
ミンBS、パーマネントレッド121%パーマネンシレ
ットIF4R、パーマネントレッドIIIRL 、バー
!ネンFレッド1■ル、パーマネントレッドν01、フ
ァスシスヵーレッ) 71)、パルカン7アストルビン
1、エオシンレーキ、ローダミンレーキ、ローダミンレ
ーキY、7リザリンレーキ、チオインジブレッドB。Colorants used in the core material include inorganic pigments, organic pigments, direct dyes, acid dyes, basic dyes, mordants, acid mordant dyes, disperse dyes, and oil-soluble dyes. Specific examples include black pigments such as carbon black, acetylene black, Larepblack, Kurofune, mineral black, aniline black, and cyanine black, and yellow pigments such as chrome yellow, zinc yellow, barium materate, and cadmium. Yellow, lead - cyanamide 1 calcium leadate ~
Su7 Thor Eo-B, Hansa Yellow 3G, Hansa Yellow 〇, Hashisa Yellow GR, Hansa Elome, Hansa Elo A-'RM1 Hansa Yellow 31 Pigment Yellow L1
Benzine Yellow, Benzine Yellow 01 Benzine Yellow O
R, Permanent Yellow NoG % Palkan 7 Ast Yellow 501 Palkan 7 Ast Yellow R1 Tartrazine Lake, Quinoline A4 Lake, Acid Yellow 5GL
s permanent erotic? GL, Permanent Yellow Ta (To), Permanent Yellow HR1 Anthravilly no Gin Yellow, etc. 1 Red pigments include red pigment, red lead, chain vermilion, cadmium red, permanent red 411, para red, fire red - vermilion, para chlorol) 2) vs. 7
x-Rin Red 1 Resolfa Cis Scarlet G1
Brilliant 7 Assis Scarlet, Brilliant 7 Carmine BS, Permanent Red 121% Permanent Silette IF4R, Permanent Red IIIRL, Bar! Nene F Red 1■ Le, Permanent Red ν01, Fasciscare) 71), Palcan 7 Astorbin 1, Eosin Lake, Rhodamine Lake, Rhodamine Lake Y, 7 Rizarin Lake, Thioin Dibred B.
チオインジゴマルーン、パーマネントレッド7G!I
s PV 力t :/ HRQ J’、青色顔料として
、群青、紺青、コバルトブルー、アルカリブルーレーキ
、ピーコックブルーレーキ、ビクトリアブルーレーキ、
無金属7タロシアニンプルー、フタロシアニンブルー、
77ストスカイブルー、インダンスレンブル−REl
sインダンスレンブル−B8、インジゴなど、があげら
れ、ざらに
黄色染料として、o、工、(カラーインデックス)ダイ
レクトイエロー98.0.工、ダイレクトイエロー89
、O,1,ダイレクトイエロー88(以上直接染料)、
0、工、アシッドイエロー1% O,X、アシッドイエ
ロー3、o、工、アシッドイエロー7(以上酸性染料)
、O,X、ベーシックイエロー1%O,工、ベーシック
イエロー2、Q、工、ベーシックイエロー11(以上1
1fit性染料) 、o、工、モダン訃イエロー26
(tl&染・酸性媒染染料) 、O,X、ディスパース
イエ” −1s0、x、ディスパースイxvs−3,0
,X、デ(Xパースイエロー4 (以上分散染料> 、
O,X、ツルベンジイエロー2.0.工、ソルベントイ
エロー6、o。Thioindigo maroon, permanent red 7G! I
s PV power t :/ HRQ J', as blue pigments, ultramarine, navy blue, cobalt blue, alkali blue lake, peacock blue lake, Victoria blue lake,
Metal-free 7 thalocyanine blue, phthalocyanine blue,
77 St. Sky Blue, Indance Tremble-REl
Indance Stremburu-B8, Indigo, etc. are mentioned, and as a rough yellow dye, O, Ko, (Color Index) Direct Yellow 98.0. Engineering, Direct Yellow 89
, O,1, Direct Yellow 88 (direct dye),
0, Engineering, Acid Yellow 1% O, X, Acid Yellow 3, o, Engineering, Acid Yellow 7 (more acidic dyes)
, O, X, Basic Yellow 1% O, Eng, Basic Yellow 2, Q, Eng, Basic Yellow 11 (or more
1fit dye), o, engineering, modern yellow 26
(tl&dye/acidic mordant dye), O,
,X,De(X Perth Yellow 4 (disperse dye>)
O, X, Tsurubenge Yellow 2.0. Solvent Yellow 6, o.
工、ソルベントイエロー14(以上油溶染料)など、赤
色染料として、0.:1.ダイレクトレッド1.0.I
。As a red dye, such as Solvent Yellow 14 (oil-soluble dye), 0. :1. Direct Red 1.0. I
.
ダイレクトレッド2、Q、X、ダイレクトレッド礁、(
以上直接染料>、O,工、アシッドレッド8.0゜1、
アシッドレッド13、C0工、アシッドレッド14、(
以上酸性染料) 、a、X、ベーシックレッド2.0、
工、ベーシックレツy14、OoX、ベーシックレッド
27(以上塩基性染料)、0.工、モダントレッド21
(媒染・酸性媒染染料)、O,!、ディスパースレッド
1%O0工、ディスパースレツ)T4、a、工、ディス
パースレッド5(以上分散染%) 、o、x、ツルベン
ジレッド1.0.工、ソルベントレッド3.0、工、ソ
ルベントレッド8 (以上油溶染料)など、青色染料と
して、a、X、ダイレクトブルー1so、x。Direct Red 2, Q, X, Direct Red Reef, (
Direct dye >, O, engineering, acid red 8.0゜1,
Acid Red 13, C0 Engineering, Acid Red 14, (
Acid dyes), a, X, Basic Red 2.0,
Engineering, Basic Lettu Y14, OoX, Basic Red 27 (all basic dyes), 0. Engineering, modern tread 21
(Mordant/Acid mordant dye), O,! , Disperse Red 1% O0 process, Disperse Red) T4, a, process, Disperse Red 5 (more than % disperse dyeing), o, x, Tsurubenge Red 1.0. As blue dyes, such as Solvent Red 3.0, Solvent Red 8 (oil-soluble dyes), a, X, Direct Blue 1so, x.
ダイレフ)ブルー6.0.工、ンイレクトブルーn(以
上直接染料)、a、工、アシッドブルー1,0゜1.7
シツrブルーフ、Q、I、7 ジアドブルー22゜C以
上酸性染料)、0・工、ベーシックプルーフ\0、X、
ベーシックブルー9、C8工、ベーシックブルー19(
以上塩基性染料)、0.工、モダントプルー48(媒染
・酸性媒染染料)、0.工、ディスパースブルー1.c
、工、ディスパースブルー3、C9工、ディスパースブ
ルー5C以上分散染料)、C1工、ソルベントブルー2
、C0工、ソルベントブルー11.0、工、ソルベント
ブルー12(以上[1染料)72ど、・があげられる。Dairef) Blue 6.0. Engineering, direct blue n (or more direct dye), a, engineering, acid blue 1.0°1.7
Shitsur Blue, Q, I, 7 Diad Blue (acidic dye above 22°C), 0, Engineering, Basic Proof \ 0, X,
Basic Blue 9, C8 Engineering, Basic Blue 19 (
basic dye), 0. Modern Plue 48 (mordant/acidic mordant dye), 0. Engineering, Disperse Blue 1. c.
, Work, Disperse Blue 3, C9 Work, Disperse Blue 5C or higher disperse dye), C1 Work, Solvent Blue 2
, C0, Solvent Blue 11.0, Solvent Blue 12 (the above [1 dye) 72, etc.].
着色剤溶液又は分散液にパラフィンワックスなどの低融
点物質や水ガラス等を、内包瞼の放出防止や多少の受像
体への結着力な与えるために添加してもよい。着色副溶
液又は分数液に占める着色剤の含有量は、0.005〜
10重量−好ましくは0.01〜5重量弧である。A low melting point substance such as paraffin wax or water glass may be added to the colorant solution or dispersion in order to prevent release of the internal eyelids or to provide some binding force to the image receptor. The content of the coloring agent in the colored sub-solution or fractional solution is 0.005~
10 weights - preferably 0.01 to 5 weight arcs.
また、第1の壁膜(内壁層)f:構成するフィルム形成
性高分子物質としては、前述の7ラビ7ゴム、ゼラチン
の他粂、コラーゲン、カゼイン、フィブリノーゲン、ヘ
モグロビン、ぼりアミノ酸、寒天、アルギン酸ソーダ、
カラゲナン、フンニャルロース、ナイリン、テト箸ン、
ポリウレタン、ボリカーボネー)、ホルマリンナフタレ
ンスルホン酸縮合物、7Rノ樹脂−フル牛ツド樹脂、シ
1Jコーン樹脂、無水マレインmeats重合体(エチ
レン、ビニルメチルエーテル)IA’)、アクリル酸、
メタクリル酸系の共重合体、ポリ塩化ビニル、〆り塩化
ビニリデン、ポリエチレン、ポリスチレン、ポリビニル
7七タール、lす7クリル7マイド1ポリビニルベンゼ
ンスルホン酸、ポリビニルアルコール、合成ゴムなどを
例示することができる。In addition, the first wall membrane (inner wall layer) f: The film-forming polymer substances that constitute the above-mentioned 7-rabbit 7-gum, gelatin shell, collagen, casein, fibrinogen, hemoglobin, stream amino acids, agar, alginic acid soda,
carrageenan, hunnyarulose, nylin, tet chopsticks,
Polyurethane, polycarbonate), formalin naphthalene sulfonic acid condensate, 7R resin-full beef resin, silicone 1J corn resin, maleic anhydride meats polymer (ethylene, vinyl methyl ether) IA'), acrylic acid,
Examples include methacrylic acid-based copolymers, polyvinyl chloride, polyvinylidene chloride, polyethylene, polystyrene, polyvinyl 7-heptadal, 7-acrylic 7-mide-1 polyvinylbenzenesulfonic acid, polyvinyl alcohol, and synthetic rubber. .
さらに、第2の壁膜(外壁膜)f:構成する合成樹脂と
してはぼりカーボネート、〆リエステル、ポリアミド、
ポリエーテル、ポリオレフィン、ポリスチレン、スチレ
ン−アクリレージ共重合体、スチレン−メタクリレート
共重合体1スチレン−エチレン系不飽和千ノオレフイン
共重合体、スチレン−ビニルエステル共重合体、スチレ
ン−ビニルエーテル共重合体、スチレン−アクリロニ)
リル共重合体、スチレン−メタ7クリロニFリル共重合
体、スチレン−7クリル7ミド共重合体、スチレン−α
−メチレン脂肪酸モノカルボン酸エステル共重合体、ス
チレン−ハロゲン化ビニリデン共重合体、ポリ酢酸ビニ
ル、又はこれらの2元又は3元以上の共重合体若しくは
これら重合体の混合物など【例示することができ水性分
散液の状態で使用される〇この合成樹脂中に混入される
磁性体にはコバルF1鉄、ニッケルのような金属、アル
電ニウム1コバルト、銅、鉄、鉛、マグネシウム、ニッ
ケル、M、Ml、金、銀、7ンチモン、ベリリウム、ビ
ス!ス、カドミウム、カルシウム、マンガン、セレン、
′チタン、タングステン、バナジウムおよびジルコニウ
ムのような金属の合金又は混合物、酸化フル之ニウム、
酸化鉄、酸化銅、酸化二ックル、酸化亜鉛、酸化ジルコ
ニウム、酸化チタンおよび酸化マグネシウムのような金
属酸化物を含む金属化合一、窒化クロムのような耐火性
窒化愉、膨化タングステンおよび炭化シリカのような炭
化物、強磁性フェライトおよびそれらの混合物などを例
示することができる。Furthermore, the second wall film (outer wall film) f: constituent synthetic resins include carbonate, polyester, polyamide,
Polyether, polyolefin, polystyrene, styrene-acrylage copolymer, styrene-methacrylate copolymer 1 Styrene-ethylenically unsaturated olefin copolymer, styrene-vinyl ester copolymer, styrene-vinyl ether copolymer, styrene- acryloni)
Lyle copolymer, styrene-meta-7cryloni-F Lyle copolymer, styrene-7cryl-7mide copolymer, styrene-α
- Methylene fatty acid monocarboxylic acid ester copolymer, styrene-vinylidene halide copolymer, polyvinyl acetate, copolymers of two or more of these, or mixtures of these polymers, etc. [Examples include: Used in the form of an aqueous dispersion 〇The magnetic substances mixed into this synthetic resin include metals such as cobal F1 iron and nickel, aluminum cobalt, copper, iron, lead, magnesium, nickel, M, Ml, gold, silver, 7inches, beryllium, bis! s, cadmium, calcium, manganese, selenium,
'Alloys or mixtures of metals such as titanium, tungsten, vanadium and zirconium, fluonium oxide,
Metal compounds including metal oxides such as iron oxide, copper oxide, nickel oxide, zinc oxide, zirconium oxide, titanium oxide and magnesium oxide, refractory nitrides such as chromium nitride, expanded tungsten carbide and silica carbide. Examples include hard carbides, ferromagnetic ferrites, and mixtures thereof.
また、この磁性体として色の鮮鋭性を良くてるために着
色磁性体を用いるのが好ましい。Further, it is preferable to use a colored magnetic material as the magnetic material in order to improve the sharpness of the color.
着色された現像剤に用いられる着色磁性体として適当な
ものには、マゼンp用としては酸化鉄(ペーガラ)、N
1表面を酸化鋼で被覆したもの、N1にカドミウム赤な
吸着せしめたちの1シアン用としてはコバルシ及びその
化合物、イエロー用としては酸化鉄、N1にカドミウム
イエローを吸着せしめたものなどがある。いずれも表面
光沢が生ずるよう析出法により微小粒子を生成したり、
粉砕後化学的な表面処理が施される。Suitable colored magnetic materials for use in colored developers include iron oxide (Pegala) and N for mazenp.
1 surface coated with oxidized steel, 1 surface coated with cadmium red adsorbed on N1, 1 cyanide coated with cobalt and its compounds, yellow coated with iron oxide, and N1 coated with cadmium yellow. In both cases, fine particles are generated using a precipitation method to produce a glossy surface.
After crushing, chemical surface treatment is applied.
この磁性体の含有量は、現像剤金量に対して加〜70重
量幅好ましくは切〜ω重量≦が適当である。The content of the magnetic material is suitably within a range of 70 to 70% by weight with respect to the amount of developer gold, preferably 50 to 70% by weight≦.
次に後者の粉体現像剤について述べる。Next, the latter powder developer will be described.
粉体現像剤とは、透明樹脂中に着色剤と磁性体あるいは
着色磁性体を分数含有させたものである。A powder developer is one in which a transparent resin contains a colorant and a fraction of a magnetic substance or a colored magnetic substance.
現像剤中に含有せしめる磁性体として、該現像剤を重ね
たとき、着色された現像剤の色を有効に選択反射せしむ
るものを用い、現像剤の樹脂として、磁性体の色【償い
増強せしむるような色をもつもの或はそのように染色ま
たは着色物体を混合せしめたものを用い、直接重ね合せ
ができるようにした。As the magnetic substance contained in the developer, one that effectively selectively reflects the color of the colored developer when the developer is stacked is used, and as the resin of the developer, the color of the magnetic substance [redemption enhancement] is used. A material with a striking color or a mixture of such dyed or colored materials was used to enable direct overlapping.
磁性体は、粒径0.5〜lOμであって、その表面は円
滑で線片状または球状であって光沢を有するものが望ま
しい。かかる粒子は、無色または着色磁性体を着色透明
樹脂あるいは染料または顔料を混入した透明樹脂中に入
れるか、磁性体表面を透明または半透明着色剤でコート
したものを無色透明樹脂あるいは磁性体の色では不充分
である場合には着色透明樹脂あるいは染料または顔料を
混入した透明樹脂中に入れて作られる。磁性体と樹脂と
の割合は重ね合せ用現像剤として用いる場合容量比圧し
て、磁性体IK対し1〜50であって、現像剤としての
粒子径は5〜20μが適当である。The magnetic material preferably has a particle size of 0.5 to 10μ, a smooth linear or spherical surface, and a glossy surface. Such particles can be prepared by placing a colorless or colored magnetic material in a colored transparent resin or a transparent resin mixed with dyes or pigments, or by coating the surface of the magnetic material with a transparent or semi-transparent coloring agent and placing it in a colorless transparent resin or a colored magnetic material. If this is insufficient, it can be made by placing it in a colored transparent resin or a transparent resin mixed with dyes or pigments. When used as a developer for overlaying, the ratio of the magnetic material to the resin is suitably 1 to 50 in volume specific pressure to the magnetic material IK, and the particle diameter of the developer is 5 to 20 .mu.m.
上述の現像剤に用いられる磁性体及び着色剤は、マイク
ロカプセル現像剤と共通であり、また、着色磁性体も同
様である。The magnetic material and coloring agent used in the above developer are the same as those in the microcapsule developer, and the colored magnetic material is also the same.
Ma[K使われる樹脂としては、フェノール、ポリ、エ
ステル、スチレン、フルキ’)−17りIJ ル、ポリ
エチレン等がある。Examples of resins used include phenol, polyester, styrene, fluorine)-17 resin, and polyethylene.
、また、2成分現像剤を用いる、場合は1現像剤に必ず
しも磁性体あるいは着色磁性体【含まなくてもよい。In addition, when a two-component developer is used, one developer does not necessarily contain a magnetic material or a colored magnetic material.
以f茶白 本発明の複写プロセスは次のように行なわれる。It is brown and white. The copying process of the present invention is performed as follows.
静電潜像形成には2通りの方法が知られているがまず1
つの方法としては導電性基体とに分光感度特性を互いK
1%にする2層の光導電層を積層した感光体に対して所
定の極性の1次帯電を行なったのち、この1次帯電の逆
極性の2次帯電を施して感光体の各光導電層K、電気2
重層をその双極モーメントが互いに逆向きとなるように
形成し、次いで原稿の光倫を照射して、原稿地肌部に対
応する部位における感光体表面電位を略0とするととも
に、各色画gIK対応する静電潜像部分を互いに逆極性
の感光体表面電位分布により形成する方法がある。There are two known methods for forming electrostatic latent images.
One method is to mutually change the spectral sensitivity characteristics of a conductive substrate and a conductive substrate.
After performing primary charging to a predetermined polarity on a photoreceptor made of two photoconductive layers laminated with a concentration of 1%, secondary charging is applied to the photoreceptor with the opposite polarity to each photoconductive layer on the photoreceptor. Layer K, electricity 2
The superimposed layers are formed so that their bipolar moments are opposite to each other, and then the original is irradiated with light to reduce the photoreceptor surface potential to approximately 0 at a portion corresponding to the background of the original, and to correspond to each color image gIK. There is a method in which an electrostatic latent image portion is formed by a photoreceptor surface potential distribution having opposite polarities.
も51つの方法としては、感光体とに記録電極を用い十
及び−の配置信号により静電潜像を形成する方法がある
。Another method is to use a recording electrode on the photoreceptor and form an electrostatic latent image using positive and negative placement signals.
と記の一方の方法により作られた静電潜像は複合現像剤
で現儂しこの儂をコロナ荷電器でコロナ帯電をせしめる
ととくより一つの極性にそろえた後、記録紙に転写、定
着させる。感光体はクリーニング器によりクリーニング
されさらに残った静電潜像を除電用コロナ荷IEaで除
去し、くり返し使用する。The electrostatic latent image created by one of the methods described above is developed with a composite developer, and after being corona-charged with a corona charger to align it to one polarity, it is transferred to recording paper and fixed. let The photoreceptor is cleaned by a cleaning device, and the remaining electrostatic latent image is removed by a charge-eliminating corona charge IEa, and the photoreceptor is used repeatedly.
以下実施例を用−11て本発明を説明する。The present invention will be explained below using Examples.
〈実施例1〉
正電荷黒色現像剤として
を混合、加熱、酵解して冷却したものな粉砕し平均粒径
15μになるように分級し、これKR動化剤としてシリ
カを0,2チ加えたものを用いた。<Example 1> A positively charged black developer was mixed, heated, fermented and cooled, then crushed and classified to have an average particle size of 15 μm, and 0.2 tsp of silica was added as a KR mobilization agent. I used something similar.
−力負帯電赤色現像剤として
均粒径15μになるように分級し、これKllll剛化
剤てシリカを0.2−加えたものを用いた。A negatively charged red developer was classified to have an average particle size of 15 μm, and 0.2 μm of silica was added thereto as a stiffening agent.
これらの現像剤を等量比に混合し、114図に示す現像
装置において現像な行なった。混合比は等量近傍が望ま
しく大きくてもそのずれが2:8を越えないことが特に
望ましい。These developers were mixed in equal proportions and developed in a developing device shown in FIG. 114. It is desirable that the mixing ratio be close to equivalence, and even if it is large, it is especially desirable that the deviation does not exceed 2:8.
鎮4図はこの発明の一実施例を示す構成略図であって、
4は記録電極で、eおよびeの記録信号5により感光体
!)、に静電潜像3を作成する。2は前記静電潜像3を
現像する現像器、6は現像剤の電荷極性をそろえるため
のコロナ荷電器、7は普通紙からなる記録紙、8は前記
記録紙、7とに転写するための転写用;ロナ荷IE器、
9は定・着用ヒータ、10 i$清掃用ファーブラシ、
11は除電用:010ナ荷電器である。Figure 4 is a schematic configuration diagram showing an embodiment of the present invention,
4 is a recording electrode, and the recording signal 5 of e and e causes the photoconductor! ), an electrostatic latent image 3 is created. 2 is a developing device for developing the electrostatic latent image 3; 6 is a corona charger for aligning the charge polarity of the developer; 7 is a recording paper made of plain paper; 8 is the recording paper; For transcription; Rona load IE device,
9 is a fixed/worn heater, 10 is an i$ cleaning fur brush,
Reference numeral 11 is a 010 charger for static elimination.
実験では、誘導体フィルムとしてδμ厚の裏面アルミ蒸
着のポリエチレンテレ7タレー)(PET)を用い、+
400 Vおよび−400Vの静電潜像4を現侭機5で
eのみを黒の5Am剤で現gIIした。In the experiment, a polyethylene tele-7 (PET) film with a thickness of δμ and aluminum vapor-deposited on the back was used as the dielectric film.
The electrostatic latent images 4 at 400 V and -400 V were developed with a developing machine 5 using a black 5Am agent.
磁気ブラシ現像器又は供給ローラとして回動するスリー
ブ2−dとその内部に固定磁石2−eと現儂四−ラとし
て回動するスリーブ2−fとその内部に静電潜像3と対
向した固定磁石2−1より構成され、現像剤を搬送し現
像するものである。A sleeve 2-d that rotates as a magnetic brush developer or a supply roller, a fixed magnet 2-e inside the sleeve 2-d, a sleeve 2-f that rotates as a fourth roller, and an electrostatic latent image 3 inside the sleeve 2-d facing each other. It is composed of a fixed magnet 2-1, and conveys the developer for development.
現像は感光体とスリーブ2−f間隙が0.3mK保持さ
れ、この状態KO,2soglF)現像剤層を送りこみ
つ〜現像ローラに目α、500H!の交流と一500v
の直流電圧を印加するととKより行なわれた。この交流
の印加が無い場合には、画僧部に赤色現像剤の混合がみ
られ、画像の鮮鋭度も低いものであった。During development, the gap between the photoconductor and the sleeve 2-f is maintained at 0.3 mK, and in this state KO, 2soglF) the developer layer is fed into the developing roller ~ α, 500H! AC and -500v
This was done by applying a DC voltage of . When this alternating current was not applied, red developer was seen mixed in the image area, and the sharpness of the image was also low.
次に、それぞれの現像剤をコロナ荷電器6で荷電してe
の極性にそろえ、その後、記録紙7に転写用コロナ荷電
器8で転写し、定着用ヒータ9により加熱して定着する
ととにより記録を行った。Next, each developer is charged with a corona charger 6 and e
After that, the image was transferred onto a recording paper 7 using a transfer corona charger 8, and was heated and fixed using a fixing heater 9, thereby recording.
また除電は、除電用コロナ荷IE器11をゼ四電位にし
て、交流:IQすを加えるととkより行った。Further, static electricity was removed by setting the static electricity removal corona charge IE device 11 to zero potential and applying alternating current (IQ) current.
■のみを黒色現俸剤で現像する場合は上記の工程を印加
する電圧を一500vから+500vK!Rえることに
よりて行なった。When developing only ■ with black developer, the voltage applied in the above process should be from -500v to +500vK! This was done by repeating.
以上説明したようKこの実施例は、感光体表面に正およ
び負の静電潜像を作成し、磁気ノ(イアス下で3#!像
剤の極性により複会現倫剤で交番電界を用いて現像し、
現像剤の極性をコロナ荷電により一つの極性にそろえ、
記録紙に転写し定着した。As explained above, in this embodiment, positive and negative electrostatic latent images are created on the surface of a photoreceptor, and an alternating electric field is used with a double-layered developer depending on the polarity of the 3#! developer under a magnetic field. Develop it,
Align the polarity of the developer to one polarity by corona charging,
It was transferred to recording paper and fixed.
したがって、高速で普通紙[2色の高品質の記録が行え
る。Therefore, high-quality recording on plain paper (two colors) can be performed at high speed.
又、転写手段として粘着転写を用いる場合にはコロナ荷
電器6.8は不要になる。Further, when adhesive transfer is used as the transfer means, the corona charger 6.8 becomes unnecessary.
〈実施例2〉 ゛
本発明では、極性の異なる静電潜像を順次現侭すること
もできるが、同時に現像することも同様にできる。こへ
では電子写真法によって作られた両極性の静電潜像の現
像の例を述べる。<Embodiment 2> In the present invention, electrostatic latent images with different polarities can be developed sequentially, but they can also be developed simultaneously. Here, we will discuss an example of developing a bipolar electrostatic latent image created by electrophotography.
[5図はこの発−の一実施例を示す構成略図である。1
3は赤色光13−8とコロナ荷電@13−bと組み合わ
せた光学系、15はコpす荷電S%14は露光系であり
、これらにより感光体1上に静電潜像3を形成する。i
は前記静電潜像3を現像する現倫器、6は現像剤の電荷
極性をそろするためのコロナ荷電器、7は普通紙からな
る記@IIi、 8は前記記録紙7上に転写するための
転写用コロナ荷電器、9は定着用ヒータ、10は清掃用
ツアーブラシ、11は除電用コロナ荷電器11− bと
白色光11−暑とを組み会わせた光学系である。[Figure 5 is a schematic diagram showing the configuration of an embodiment of this generator. 1
3 is an optical system combining red light 13-8 and corona charge @ 13-b, 15 is a cop charge S% 14 is an exposure system, and these form an electrostatic latent image 3 on the photoreceptor 1. . i
is a developing device for developing the electrostatic latent image 3; 6 is a corona charger for aligning the charge polarity of the developer; 7 is a record @IIi made of plain paper; 8 is for transferring onto the recording paper 7. 9 is a heater for fixing, 10 is a tour brush for cleaning, and 11 is an optical system combining a corona charger 11-b for static elimination and a white light 11-b.
静電潜像の形成方法は以下のようにして行なった。The electrostatic latent image was formed as follows.
アルミニウム板を導電性基体とし、この上KM度99.
99−のセレンな厚さ12μに蒸着した。このセレン層
上にポリビニルカルバゾル−トリニトロフルオレノンを
厚さ18μにコーティングした。ポリビニルカルバゾル
とトリニトロフルオレノンi;f)混合比は、ポリビニ
ルカルバゾルの単位モノff −に対シ、トリニトロフ
ルオレノン0.1モルの割合であるセレン層、、ポリビ
ニルカルバゾル−トリニトロフルオレノン層(以下OP
C層と略記する)、はともに両極帯電性であり、OF2
層は半透明である。An aluminum plate is used as a conductive base, and the KM degree is 99.
99-90% selenium was deposited to a thickness of 12 μm. On this selenium layer, polyvinylcarbazole-trinitrofluorenone was coated to a thickness of 18 μm. Polyvinyl carbazole and trinitrofluorenone i; f) The mixing ratio is 0.1 mole of trinitrofluorenone per mono ff - unit of polyvinyl carbazole.Selenium layer, polyvinyl carbazole-trinitrofluorenone layer (OP below)
(abbreviated as C layer) are both polar chargeable, and OF2
The layer is translucent.
この感光体1&13−+a、東芝社製赤色フィルター−
VR64Kよって得た赤色光で均一露光しながら′、+
6.OKVノ=y o +荷11i13− b K
J: リ+700 V。This photoreceptor 1 & 13-+a, Toshiba red filter-
While uniformly exposing with red light obtained by VR64K,
6. OKVノ=y o +load 11i13- b K
J: Re+700V.
K1次帯電し、ついで暗中にて、−5,2KVのコロナ
荷電器で、−400Vまで帯電した◎ついで、露光系1
4により白地に赤色iii*および黒色画倫を有する原
稿の光像で露光を行なったところ、原稿白地部に対応す
る部位における感光体表面電位は一30V、赤色画侭A
色tiiii倫に対応する静電潜像部分は、それぞれ+
300 V、 −400Vの感光体表面電位分布により
静電潜像が形成された。K primary charging, then charging to -400V with a -5.2KV corona charger in the dark ◎Next, exposure system 1
When exposure was carried out using a light image of a document having red iii* and black image lines on a white background according to 4, the photoreceptor surface potential at the part corresponding to the white background of the document was -30V, and the red image side A.
The electrostatic latent image portion corresponding to color tiii is +
An electrostatic latent image was formed with a photoreceptor surface potential distribution of 300 V and -400 V.
これを磁気ブラシ現像器2において実施例1で用いた複
合現像剤で現像した。磁気ブラシ現像器2は供給ローラ
として回動するスリーブ2−dとその内部に固定磁石2
−e、現儂四−ラとして回動する2本のスリーブ2−f
とその内部に静電潜像3と対向した固定磁石2−gより
構成され現像剤を搬送し現像するものである。現像は感
光体lとスリーブ5−111ffが0.3mK保持さレ
コノ状3IAK O,4ymの現像剤層を送りこみつ〜
各々の現像ローラに0.4KV 1500 Hzの交流
と±soo vの直流電圧を印加することにより行なわ
れた。この交流の印加がない場合には、iii儂に黒色
現像剤と赤色現像剤の混合がみられ画像の鮮鋭度も低い
ものであった。次にそれぞれの現像剤をコロナ荷電gS
6で荷電してeの極性にそろえ、その後、記録紙7に転
写用コロナ荷電lI8で転写し、定着用ヒータ9により
加熱して定着することにより記録を行った。また除電は
、除電用コロナ荷電l9111’ゼロ電位にして、交流
コロナと白色光を加えることKより行った。This was developed using the composite developer used in Example 1 in a magnetic brush developer 2. The magnetic brush developing device 2 includes a sleeve 2-d that rotates as a supply roller and a magnet 2 fixed inside the sleeve 2-d.
-e, two sleeves 2-f rotating as the current four-ra
It is comprised of a fixed magnet 2-g which faces an electrostatic latent image 3 inside thereof, and conveys the developer for development. For development, the photoconductor L and sleeve 5-111ff are held at 0.3 mK and a developer layer of 3IAK O, 4ym is fed into the photoreceptor.
This was carried out by applying a 0.4 KV 1500 Hz alternating current and a ±soo v direct current voltage to each developing roller. When this alternating current was not applied, a mixture of black developer and red developer was observed, and the sharpness of the image was also low. Next, each developer is corona charged with gS
6 to align the polarity with e, and then transferred to a recording paper 7 with a transfer corona charge lI8, and was heated and fixed by a fixing heater 9 to perform recording. Further, static elimination was performed by setting the static elimination corona charge l9111' to zero potential and applying an alternating current corona and white light.
以上、説明したように実施例2では感光体表面に正およ
び負の静電潜像を作成しかぶりを防ぐ磁気バイアス下で
、現像剤の極性により複合現像剤で画倫を改良する交番
電界を用いて現像し、現像剤の極性をコロナ荷電により
一つの極性にそろえ、記録紙に転写し定着した。従って
、高速で普通紙に2色の高品質の記録が行える利点があ
る。As explained above, in Example 2, positive and negative electrostatic latent images are created on the surface of the photoreceptor under a magnetic bias that prevents fogging, and an alternating electric field is applied to improve image quality with a composite developer depending on the polarity of the developer. The polarity of the developer was adjusted to one polarity by corona charging, and the developer was transferred and fixed onto recording paper. Therefore, there is an advantage that high-quality two-color recording can be performed on plain paper at high speed.
又、転写手段として粘着転写を用いる場合には。Also, when adhesive transfer is used as the transfer means.
コロナ荷電器6〜8は不要になる。The corona chargers 6 to 8 become unnecessary.
第1図は静電潜像の電位と現像剤量との関係を示すグラ
フ、第2図、第3図は本発明の現像器の概略構成図、第
4図、第5図は本発明の詳細な説明する概略構成図であ
る。
」は感光体、2は現像器、3は静電温償、4は記録電極
、5は記録信号、6はコロナ荷電器、7は記録紙、8は
転写用コロナ荷電器、9は定着用ヒータ、 10は清掃
用ファーブラシ、11は除電用コロナ荷電器J2は交流
電源、13は光学系。
代理人桑原義美
も 1 口
帖2図
2二〇 4
躬 4 図
手続補正書
1 ′ドI’lの衣小
昭和56;I持請願第 150147 リ2 発明の
名称
静電荷儂現倫方法
:) 補市をする古
・lfイ′1との関係 特許出願人
イ1 所 東5;七都新宿区西新11・i l i’
lI’26番2ぢ名 称 (+271小西六″)J:
貞[′、業株式会拐代表取締役 川 本 信 彦
5 補III旬令の11イj 自 発6、補正の対象
(1)図面第3図および第5図■)明細書の「発明
の詳細な説明」の欄7、 補正の内容
(1) 図面の訂正
別紙の通り
(2)明細書中の補正
第潤頁19行目「静電漕g14」とあるを「静電温償3
」と訂正。
同頁加行目「現情機5」とあるな「現#I器2」と訂正
。
第25頁19行目「黒色現倫剤」とあるを「赤色現倫剤
」と訂正。
wE28頁3行目「帯電器で、」とあるな「帯電器15
で、」と訂正。FIG. 1 is a graph showing the relationship between the potential of an electrostatic latent image and the amount of developer, FIGS. 2 and 3 are schematic diagrams of the developing device of the present invention, and FIGS. FIG. 2 is a schematic configuration diagram for detailed explanation. '' is a photoreceptor, 2 is a developing device, 3 is an electrostatic temperature compensator, 4 is a recording electrode, 5 is a recording signal, 6 is a corona charger, 7 is a recording paper, 8 is a corona charger for transfer, 9 is for fixing 10 is a fur brush for cleaning, 11 is a corona charger J2 for static elimination, is an AC power source, and 13 is an optical system. Agent Yoshimi Kuwabara 1. Album 2 Figure 220 4. 4. Amendment to figure procedure 1 'Do I'l's clothes Koro Showa 56; Relationship with old/lf I'1 which is a supplementary market Patent applicant I1 Location Higashi 5; Shichito Shinjuku-ku Nishishin 11 I l i'
lI'26 No. 2 Name (+271 Konishi 6") J:
Nobuhiko Kawamoto, Representative Director of the Company Limited Supplement III Act, Vol. Column 7, "Explanation" Contents of the amendment (1) Correction of the drawings As shown in the attached sheet (2) In the specification, the words "electrostatic tank g14" on the 19th line of the first page of the amendment have been replaced with "electrostatic thermal compensation 3"
” and corrected. The third line on the same page, which says ``Genjoki 5,'' has been corrected to ``Genuine #I 2.'' On page 25, line 19, the text ``black genrenji'' has been corrected to ``red genrinji.'' wE page 28, line 3, it says, ``With a charger,'' ``Charger 15.
So,” he corrected.
Claims (1)
一方の極性に帯電された着色粒子を選択的に抽出し、抽
出された着色粒子で像支持体上の異なる極性の静電潜像
の一方の極性の静電潜像を現像することを特徴とする静
電荷像現像方法。 (り 上記着色粒子が磁性体を含有することを特徴とす
る特許請求の範囲第1項記載の静電荷像現像方法。 (濠 上記着色粒子の抽出に交番電界を用いることを特
徴とする特許請求の範囲第1項又は第2項記載の静電荷
像現像方法。 (4上記着色粒子は互いに異なった色に着色されている
ことを特徴とする特許請求の範囲at項、第2項又i裏
第3項記載の静電荷像現像方法。 (均 上記着色粒子の現像に交番電界を用いることを特
徴とする特許請求の範囲第1項、第2項、第3項又は第
4項記載の静電荷像現像方法。 (6) 上記互いに異なる帯電極性と有する着色粒子
の現像が同時に行なわれることを特徴とする特許請求の
範囲第1項、第2項、第3項、第4項又は第5項記載の
現像方法。 σ) 上記互いに異なる帯電極性と有する着色粒子は帯
電極性を除ぎ現gI!に寄与するノ(ラメークが実質的
に同じであることを特徴とする特許請求の範囲第1項、
第2項、第3項、第4項、第5項又は第6項記載の現像
方法。[Claims] (1) Colored particles charged to one polarity are selectively extracted from colored particles having different charge polarities, and the extracted colored particles are used to charge electrostatic charges of different polarity on an image support. An electrostatic charge image developing method characterized by developing an electrostatic latent image of one polarity of the latent image. (ri) A method for developing an electrostatic image according to claim 1, characterized in that the colored particles contain a magnetic substance. The method for developing an electrostatic image according to claim 1 or 2.(4) The above-mentioned colored particles are colored in different colors. A method for developing an electrostatic image according to claim 3. (Evening method) Charged image developing method. (6) Claims 1, 2, 3, 4, or 5, characterized in that the development of the colored particles having different charging polarities is performed simultaneously. The developing method according to claim 1. σ) The colored particles having charge polarities different from each other contribute to the development gI! except for the charge polarity. section,
The developing method according to item 2, 3, 4, 5, or 6.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56150147A JPS5850548A (en) | 1981-09-21 | 1981-09-21 | Electrostatic image developing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56150147A JPS5850548A (en) | 1981-09-21 | 1981-09-21 | Electrostatic image developing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5850548A true JPS5850548A (en) | 1983-03-25 |
| JPH0237595B2 JPH0237595B2 (en) | 1990-08-24 |
Family
ID=15490516
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56150147A Granted JPS5850548A (en) | 1981-09-21 | 1981-09-21 | Electrostatic image developing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5850548A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60126658A (en) * | 1983-12-13 | 1985-07-06 | Fujitsu Ltd | Developing method |
| JPS60131554A (en) * | 1983-12-20 | 1985-07-13 | Konishiroku Photo Ind Co Ltd | Toner image forming method |
-
1981
- 1981-09-21 JP JP56150147A patent/JPS5850548A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60126658A (en) * | 1983-12-13 | 1985-07-06 | Fujitsu Ltd | Developing method |
| JPS60131554A (en) * | 1983-12-20 | 1985-07-13 | Konishiroku Photo Ind Co Ltd | Toner image forming method |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0237595B2 (en) | 1990-08-24 |
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